Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "F"

421 to 430 of 433 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
421	93986	FOXP2	Forkhead box P2	CAGH44, SPCH1, TNRC10	7q31 microdeletion syndrome, Adenocarcinoma, Apraxia, Attention deficit hyperactivity disorder, Auditory processing disorder, Autism, Diabetes, Diabetes mellitus, Dysarthria, Endometriosis, Gastroesophageal reflux disease, Grammar-specific speech disorder, Language development disorders, Mental depression, Narcolepsy View all (8 more)
422	9415	FADS2	Fatty acid desaturase 2	D6D, DES6, FADSD6, LLCDL2, SLL0262, TU13	Alopecia, Asthma, Atrial fibrillation, Bipolar disorder, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Coronary heart disease, Crohn disease, Depressed bipolar disorder, Diabetes, Diabetes mellitus, Heart failure, Hypothyroidism, Inflammatory bowel disease View all (12 more)
423	94234	FOXQ1	Forkhead box Q1	HFH1	Breast cancer, Mammary neoplasms, Breast carcinoma, Marfan syndrome
424	9457	FHL5	Four and a half LIM domains 5	1700027G07Rik, ACT, FHL-5, dJ393D12.2	Abdominal migraine, Common migraine, Confusional migraine, Coronary artery disease, Hemicrania migraine, Migraine, Status migrainosus
425	9637	FEZ2	Fasciculation and elongation protein zeta 2	HUM3CL	Myocardial ischemia
426	9638	FEZ1	Fasciculation and elongation protein zeta 1	UNC-76	Attention deficit hyperactivity disorder, Bipolar disorder, Development disorder, Mental depression, Psychosis, Schizophrenia, Vascular diseases
427	96459	FNIP1	Folliculin interacting protein 1	IMD93	Alzheimer disease
428	9679	FAM53B	Family with sequence similarity 53 member B	KIAA0140, bA12J10.2, smp	Alopecia, Alopecia, male pattern, Androgenetic alopecia
429	9758	FRMPD4	FERM and PDZ domain containing 4	MRX104, PDZD10, PDZK10, XLID104	Attention deficit hyperactivity disorder, Autism, Cerebral cortical atrophy, Developmental delay, Facial paralysis, Neurosensory hearing impairment, High palate, Hypoplasia of corpus callosum, Mental retardation, Macrocephaly, Meckel diverticulum, Mental retardation, x-linked, Non-syndromic intellectual disability, x-linked, Nystagmus, Obesity View all (4 more)
430	9855	FARP2	FERM, ARH/RhoGEF and pleckstrin domain protein 2	FIR, FRG, PLEKHC3	2q37 deletion syndrome, Autism, Lymphocytic leukemia, Nasopharyngeal carcinoma, Prostate cancer, Vitiligo

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